Found: 22
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The Hemarthrosis-Simulating Knee Model: A Useful Tool for Individualized Education in Patients with Hemophilia (GEFACET Study).
- Published in:
- Journal of Blood Medicine, 2021, v. 12, p. 133, doi. 10.2147/JBM.S280032
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- Publication type:
- Article
Effectiveness of long‐term prophylaxis using pdFVIII/VWF concentrate in patients with inherited von Willebrand disease.
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- European Journal of Haematology, 2022, v. 109, n. 1, p. 109, doi. 10.1111/ejh.13778
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- Article
Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort.
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- British Journal of Haematology, 2020, v. 188, n. 2, p. 317, doi. 10.1111/bjh.16133
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- Article
Comparison of one‐stage and chromogenic factor VIII assays to tailor the dose of recombinant factor VIII‐Fc fusion protein (rFVIIIFc, efmoroctocog alfa) in adult patients with haemophilia A: Single‐centre, real‐world experience of surgery
- Published in:
- Haemophilia, 2024, v. 30, n. 2, p. 538, doi. 10.1111/hae.14929
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- Publication type:
- Article
Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross‐sectional study based on the FranceCoag registry.
- Published in:
- Haemophilia, 2023, v. 29, n. 5, p. 1202, doi. 10.1111/hae.14841
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- Article
A focus on dominant negative variants in a series of 170 heterozygous FXI‐deficient patients.
- Published in:
- Haemophilia, 2023, v. 29, n. 4, p. 1113, doi. 10.1111/hae.14802
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- Article
Report of surgeries, their outcome and the thrombin generation assay in patients with Factor XI deficiency: A retrospective single‐centre study.
- Published in:
- Haemophilia, 2022, v. 28, n. 2, p. 301, doi. 10.1111/hae.14506
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- Publication type:
- Article
Management of intracranial haemorrhage in a newborn with inherited factor VII deficiency with the use of rFVIIa aliquots.
- Published in:
- Haemophilia, 2021, v. 27, n. 4, p. e487, doi. 10.1111/hae.14199
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- Publication type:
- Article
Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX.
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- Haemophilia, 2021, v. 27, n. 4, p. e462, doi. 10.1111/hae.14146
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- Publication type:
- Article
Haemophilia A patients' medication adherence to prophylaxis with efmoroctocog alfa.
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- Haemophilia, 2021, v. 27, n. 3, p. e368, doi. 10.1111/hae.14301
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- Publication type:
- Article
Management of previously untreated patients with severe haemophilia A preferentially treated with recombinant factor VIII products: Two French centres' real‐life experience.
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- Haemophilia, 2020, v. 26, n. 6, p. e349, doi. 10.1111/hae.14132
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- Publication type:
- Article
Benefits of thromboelastometry for monitoring replacement therapy in patients with severe inherited factor XIII deficiency: 3 illustrative cases.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. e336, doi. 10.1111/hae.13823
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- Publication type:
- Article
Intramuscular vaccination of haemophiliacs: Is it really a risk for bleeding?
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- Haemophilia, 2019, v. 25, n. 5, p. e322, doi. 10.1111/hae.13808
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- Publication type:
- Article
A single‐centre study of management of pregnant women with von Willebrand disease.
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- 2019
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- Publication type:
- Letter to the Editor
Anterior segment dysgenesis in a child with factor VII deficiency.
- Published in:
- Clinical Ophthalmology, 2007, v. 1, n. 3, p. 335
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- Publication type:
- Article
Déficit congénital en facteur XIII en 2020 Prévalence, diagnostic clinique et biologique et modalités thérapeutiques.
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- Hematologie, 2020, v. 26, n. 4, p. 192, doi. 10.1684/hma.2020.1571
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- Publication type:
- Article
Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene: A Secondary Analysis of a Phase 1/2 Clinical Trial.
- Published in:
- 2019
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- Publication type:
- journal article
GGCX‐related congenital combined vitamin K‐dependent clotting factors deficiency‐1: Description of a fetus with chondrodysplasia punctata.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 1, p. 314, doi. 10.1002/ajmg.a.62503
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- Publication type:
- Article
Severe haemorrhages leading to a diagnosis of rare bleeding disorder occur at a very young age: A study from the FranceCoag network.
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- Haemophilia, 2024, v. 30, n. 4, p. 981, doi. 10.1111/hae.15033
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- Publication type:
- Article
Quality of life of siblings of adolescents with severe haemophilia (FRATHEMO): An ancillary study to the TRANSHEMO project.
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- Haemophilia, 2024, v. 30, n. 4, p. 1071, doi. 10.1111/hae.15023
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- Publication type:
- Article
Stromal cell‐derived factor 1 alpha (SDF‐1alfa) and cartilage oligomeric matrix protein (COMP): Two potential signature biomarkers of radiological detectable hemophilic arthropathy.
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- International Journal of Rheumatic Diseases, 2024, v. 27, n. 2, p. 1, doi. 10.1111/1756-185X.15061
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- Publication type:
- Article
SHORT REPORT Two novel factor V null mutations associated with activated protein C resistance phenotype/genotype discrepancy.
- Published in:
- British Journal of Haematology, 2003, v. 123, n. 2, p. 342, doi. 10.1046/j.1365-2141.2003.04620.x
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- Publication type:
- Article